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Constructivist Prenatal Education Effects

The Effect of a Constructivist-Based Prenatal Education Program on Pregnant Women's Fear of Childbirth, Pain Beliefs, and Self-Efficacy for Normal Delivery: A Randomized Controlled Trial.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07268027
Enrollment
126
Registered
2025-12-05
Start date
2025-12-01
Completion date
2026-03-01
Last updated
2026-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childbirth Education, Fear of Childbirth, Pain, Self-Efficacy

Keywords

Pregnancy Education Program, Fear of Childbirth, Pain Belief, Self-Efficacy for Normal Birth

Brief summary

The Effect of a Constructivist-Based Prenatal Education Program on Pregnant Women's Fear of Childbirth, Pain Beliefs, and Self-Efficacy for Normal Delivery: A Randomized Controlled Trial.

Detailed description

The study is a randomized controlled trial. It will be conducted at the prenatal school of Konya City Hospital between December 2025 and May 2026. A total of 126 primiparous pregnant women will be included in the study (intervention group n=63, control group n=63). The intervention group will receive the Constructivist-Based Prenatal Education Program, while the control group will receive the standard prenatal care and education provided by the hospital. Data will be collected using a personal information form, the Fear of Childbirth Scale, the Pain Beliefs Scale, and the Self-Efficacy for Normal Birth Scale.

Interventions

OTHERConstructivist-Based Prenatal Education Group

Pregnant women who agree to participate in the study and are assigned to the childbirth preparation education group will receive a Constructivist-Based Prenatal Education Program in the prenatal school department of the hospital for a total of 24 hours over 3 days. Participants in the intervention group will attend the classes in groups of 15.

Sponsors

Selcuk University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Registered in the hospital's prenatal school and actively participating in the 3-day training sessions, * Aged 18 years or older, * Between 20 and 32 weeks of gestation, * Having a singleton and low-risk pregnancy, * Primiparous (expecting their first birth), * Voluntarily agreeing to participate by signing the written informed consent form, * Able to read, understand, and communicate in Turkish.

Exclusion criteria

* Those who have previously given birth vaginally or by cesarean section (multiparous women), * Those with multiple pregnancies, * Those who conceived through assisted reproductive techniques, * Those diagnosed with serious obstetric or medical complications during pregnancy (such as preeclampsia, gestational diabetes, or risk of preterm birth), * Those with a history of psychiatric diagnosis or currently receiving psychiatric treatment, * Foreign nationals.

Design outcomes

Primary

MeasureTime frameDescription
Comparison of the sociodemographic characteristics of pregnant women before the training with a survey.6 monthsSociodemographic information of pregnant women will be collected through surveys, compared, and reported.
Comparison of obstetric characteristics of pregnant women before the training with a questionnaire.6 monthsObstetric data of pregnant women will be collected through questionnaires, compared, and reported.
Comparison of the means of the Fear of Childbirth Scale among pregnant women across groups.6 monthsThe Fear of Childbirth Scale will be administered to pregnant women. The Respectful Childbirth Care scale ranges from 0 to 160 points (min-max), with higher scores indicating higher fear of childbirth.
Comparison of the Pain Beliefs Scale means among pregnant women across groups.6 monthsThe Pain Beliefs Scale will be administered to pregnant women.The scale evaluates two types of pain-related beliefs: organic and psychological. It includes 12 items rated on a 6-point Likert scale, with 8 items assessing organic beliefs (pain as a physiological or pathophysiological condition) and 4 items assessing psychological beliefs (pain influenced by anxiety, depression, or external factors). No total score is calculated; each subscale score is the mean of its items. Higher scores indicate stronger beliefs in that specific dimension.
Comparison of mean scores on the Self-Efficacy Scale for Normal Childbirth among pregnant women across groups.6 monthsThe Self-Efficacy Scale for Normal Childbirth will be administered to pregnant women. Possible scores on the scale are 0-90 (min-max). Higher scores indicate higher self-efficacy levels.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 27, 2026